関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulmazole | HCID 5353 | — |
| 反応物 | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| 反応物 | L-Ascorbic Acid | HCID 54670067 | — |
| 触媒 | Ferrous Sulfate | HCID 24393 | — |
| 溶媒 | Hydrogen Peroxide | HCID 784 | — |
| 溶媒 | Phosphate | HCID 1061 | — |
| 生成物 | 2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridine | HCID 13036815 | — |
反応手順
7.2 gm of 2-(2-methoxy-4-methylsulfinyl-phenyl)-1H-imidazo[4,5-b]pyridine were dissolved in a mixture of a phosphate buffer of pH 7.2 and 120 ml of 3% hydrogen peroxide, and a solution of 9.3 gm of ethylenediamine tetraacetic acid, 4.4 gm of ascorbic acid, 3.8 gm of iron(II) sulfate in a phosphate buffer of pH 7.2 was added. After 30 minutes the reaction mixture was evaporated in vacuo, and the residue was purified by chromatography on a polystyrene resin column (XAD-2 of Rohm & Haas) with water and methanol as eluants. After evaporation of the eluate the two compounds were separated by means of chromatography on silicagel [eluant: chloroform/methanol/ammonia water=85/15/2 (v/v)]. 2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridine was obtained as yellow powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04353909 |
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| 出典データセット | uspto-grants-1982_10 |
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| ORD ID | ord-82029858ee1c4b3dbc75f90598e80ee4 |
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| 出典メモ | uspto-grants-1982_10 |
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